FDA UDI In Commercial Distribution 🇺🇸 United States

BONE-LOK MVP Cortical-Cancellous Compression Device

DI: 81195401192562 · Model: TMCD-35-4050S · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BONE-LOK MVP Cortical-Cancellous Compression Device
Primary DI
81195401192562
Version / Model
TMCD-35-4050S
Catalog Number
9022-02
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
53d98d7b-f18d-499d-9076-e3a22831fbcd

Device Description

3.5mm Diameter x 40-50mm Length

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 81195401192562

Customer Contacts

Phone
800-497-0484